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超臨界二酸化炭素によるポリ酢酸ビニルおよびポリスチレン中からのベンゼンの抽出

https://hiroshima.repo.nii.ac.jp/records/2010274
https://hiroshima.repo.nii.ac.jp/records/2010274
37bdff07-5d52-4386-ae79-c5b60a43ec8b
名前 / ファイル ライセンス アクション
JJpnPetrolInst_32_67.pdf JJpnPetrolInst_32_67.pdf (1.0 MB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル 超臨界二酸化炭素によるポリ酢酸ビニルおよびポリスチレン中からのベンゼンの抽出
言語 ja
タイトル
タイトル Supercritical Carbon Dioxide Extraction of Benzene in Poly(vinyl acetate) and Polystyrene
言語 en
作成者 佐々木, 正和

× 佐々木, 正和

ja 佐々木, 正和

en Sasaki, Masakazu

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滝嶌, 繁樹

× 滝嶌, 繁樹

ja 滝嶌, 繁樹

en Takishima, Shigeki

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舛岡, 弘勝

× 舛岡, 弘勝

ja 舛岡, 弘勝

en Masuoka, Hirokatsu

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 Copyright (c) 1989 (社)石油学会
権利情報
権利情報 本文データはJournal@rchiveから複製したものである
主題
主題Scheme Other
主題 Benzene
主題
主題Scheme Other
主題 Carbon dioxide
主題
主題Scheme Other
主題 Diffusion
主題
主題Scheme Other
主題 Mass transfer
主題
主題Scheme Other
主題 Polymer
主題
主題Scheme Other
主題 Supercritical fluid extraction
主題
主題Scheme NDC
主題 570
内容記述
内容記述 超臨界二酸化炭素を抽剤とし, ポリ酢酸ビニルおよびポリスチレンの二種類のポリマー中からのベンゼンの分離実験を行い, 超臨界流体抽出法の適用性を検討した。従来から行われている代表的な分離法である真空ストリッピング法に比べて, 超臨界流体抽出法では, 比較的低い操作温度下で短時間に低濃度まで, ポリマー中よりベンゼンを除去することが可能であった。また, この抽出実験データを単純な物質移動モデルに基づいて整理したところ, ベンゼンの物質移動速度の増進の原因は, ポリマー中へ二酸化炭素が溶解し, ポリマー中のベンゼンの拡散係数が増大したことによるものであることがわかった。
言語 ja
内容記述
内容記述 In order to test the applicability of the supercritical fluid extraction technique to the separation of impurities in polymers, separation of benzene from two polymers of poly(vinyl acetate) and polystyrene was carried out using supercritical carbon dioxide. Figure 1 shows a schematic diagram of the supercritical fluid extraction apparatus. It consists of the following sections: (1) compression of carbon dioxide, (2) extraction, and (3) control and measurement of carbon dioxide flow rates. A sample polymer disk of known dimensions which had dissolved a known quantity of benzene, was placed in the extraction cell. The concentration of benzene in the sample polymer before and after extraction was determined using a gas chromatograph. Table 1 gives the conditions used in the experiments. Vacuum stripping (a conventional separation method) was performed along with the supercritical fluid extraction method for the benzene+poly(vinyl acetate) system. It appeared that the supercritical fluid extraction method was able at near room temperature to remove benzene more rapidly and to lower concentrations than vacuum stripping, as shown in Figures 2 and 3. The flow rate of carbon dioxide had but slight influence, under the conditions used, on the experimental results. Hence, if the mass transfer resistance of benzene is separated into two parts, i.e., one in polymer phase and the other in the supercritical carbon dioxide phase, it is evident that the mass transfer of benzene is controlled by the polymer phase (Figs. 4, 5). Extraction experiments were carried out varying initial concentration of benzene in poly(vinyl acetate); the results seemed but little affected by varying the initial concentration (Fig. 6). Extraction experiments were also carried out with samples of different thicknesses in the poly(vinyl acetate) system. After 55 minutes the yield of extraction increased up to 99.8% at 313K and 7.95MPa when the sample thickness was 0.5mm. However, the yield decreased with increasing sample thickness (Figs. 7, 8). The experimental results after 1h at temperature range of 300-373K and pressures of 7.95MPa and 14.8MPa are shown in Figure 9. The rate of extraction of poly(vinyl acetate) system was much greater than that of the polystyrene system. As for the effect of pressure, extraction at 14.8MPa could be performed with a greater rate than at 7.95MPa; on the other hand, the effect of temperature seemed rather complex. Yields of extraction of the poly(vinyl acetate) system at 7.95MPa and 14.8MPa increased with increasing temperature. The experimental results of the polystyrene system at 14.8MPa showed a tendency similar to that of the poly(vinyl acetate) system. However, the experimental results of the polystyrene system exhibited a minimum at 343K and at 7.95MPa. The diffusion coefficient of benzene in polymers in the presence of supercritical carbon dioxide was evaluated from the experimental data by using a simple mass transfer model (Figs. 10, 12). The calculated diffusion coefficient of benzene in poly(vinyl acetate) was found to be about midway between the value in supercritical carbon dioxide and that in poly(vinyl acetate) in the absence of supercritical carbon dioxide (Fig. 11). The calculated diffusion coefficient was more than 6 orders larger than that in poly(vinyl acetate) in the absence of supercritical carbon dioxide. This was the consequence of dissolution of supercritical carbon dioxide into the polymer.
言語 en
出版者
出版者 石油学会
言語
言語 jpn
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ URI
関連識別子 http://www.journalarchive.jst.go.jp/japanese/jnlabstract_ja.php?cdjournal=jpi1958&cdvol=32&noissue=2&startpage=67
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0582-4664
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AN00130954
開始ページ
開始ページ 67
書誌情報 石油学会誌
石油学会誌

巻 32, 号 2, p. 67-74, 発行日 1989-03-01
旧ID 30497
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